Christina Gurnett

Medicine & Life Sciences

1. Clubfoot 100%
2. Scoliosis 64%
3. Mutation 44%
4. Genes 35%
5. Epilepsy 28%
6. Flatfoot 26%
7. Arthrogryposis 25%
8. Distal type 1 Arthrogryposis multiplex congenita 18%
9. Skeletal Muscle 18%
10. Phenotype 16%
11. Zebrafish 15%
12. Single Nucleotide Polymorphism 13%
13. Exome 12%
14. Child 11%
15. Seizures 11%
16. Human Genetics 11%
17. Muscles 10%
18. Chromosomes 10%
19. Intellectual Disability 9%
20. Foot 9%
21. Autistic Disorder 9%
22. Contracture 9%
23. Partial Epilepsy 8%
24. Extremities 8%
25. Pedigree 8%
26. myosin-binding protein C 8%
27. Conotoxins 8%
28. Filamins 8%
29. Genome 8%
30. Myosins 7%
31. Genome-Wide Association Study 7%
32. Calcium Channels 7%
33. Myosin Heavy Chains 6%
34. Kinesin 6%
35. Carrier Proteins 6%
36. Polydactyly 6%
37. Chloride Channels 6%
38. Developmental Disabilities 6%
39. Triphalangeal Thumb 6%
40. Syringomyelia 6%
41. Disabled Children 6%
42. Growth Differentiation Factor 5 6%
43. Joint Instability 6%
44. Chromosome Duplication 5%
45. Voltage-Gated Potassium Channels 5%
46. Congenital, Hereditary, and Neonatal Diseases and Abnormalities 5%
47. Xenopus 5%
48. Whole Exome Sequencing 5%
49. Missense Mutation 5%
50. Hand 5%